阴蒂迷离瘤：一例罕见病例报告
Clitoral Choristoma: A Rare Case Report.
作者信息
Aihole Jayalaxmi Shripati, Lokanath Hemalatha, Babu M Narendra, Deepak J
机构信息
Department of Paediatric Surgery, IGICH, Bengaluru, Karnataka, India.
Department of Pathology, IGICH, Bengaluru, Karnataka, India.
出版信息
J Indian Assoc Pediatr Surg. 2017 Jul-Sep;22(3):163-164. doi: 10.4103/0971-9261.207642.
Abstract
Clitoral hypertrophy is usually seen as a congenital malformation, specifically during the stages of hormonal expressions in the disorders of sexual development. Acquired clitoral hypertrophy is a relatively rare condition. Clitoris can be the site of neoplastic lesions. Clitoral choristoma has not been reported so far in the literature.
摘要
阴蒂肥大通常被视为一种先天性畸形，特别是在性发育障碍中激素表达阶段出现。后天性阴蒂肥大是一种相对罕见的情况。阴蒂可能是肿瘤性病变的部位。阴蒂迷芽瘤目前在文献中尚未见报道。
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